T. Horikoshi

Peripheral Quantitative Computed Tomography of the Femoral Neck in 60 Japanese Women

H. Takahashi, T. Horikoshi, N. Endo, 1999, Calcified Tissue International.

A large-scale genetic association study of ossification of the posterior longitudinal ligament of the spine

H. Baba, Kozo Nakamura, M. Matsumoto, 2006, Human Genetics.

Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly

Naoto Endo, Peter Heutink, Minoru Shibata, 2002, Proceedings of the National Academy of Sciences of the United States of America.

MATN and LAPTM are parts of larger transcription units produced by intergenic splicing: intergenic splicing may be a common phenomenon.

Y. Miyamoto, S. Ikegawa, A. Mabuchi, 2006, DNA research : an international journal for rapid publication of reports on genes and genomes.

Mutation in the von Willebrand factor‐A domain is not a prerequisite for the MATN3 mutation in multiple epiphyseal dysplasia

S. Ikegawa, A. Mabuchi, E. Nakashima, 2005, American journal of medical genetics. Part A.

Coxsackievirus and adenovirus receptor (CAR)-positive immature osteoblasts as targets of adenovirus-mediated gene transfer for fracture healing

R. Kuwano, T. Ito, H. Katagiri, 2003, Gene Therapy.

Characterization of Osteoblast Progenitor Cells in Human Iliac Bone Marrow

T. Horikoshi, N. Endo, T. Tanizawa, 1999 .

Disruption of the C7orf2/Lmbr1 genic region is associated with preaxial polydactyly in humans and mice

P. Heutink, S. Noji, T. Horikoshi, 2003, Journal of Bone and Mineral Metabolism.